Retinoblastoma in a patient with a 13qXp translocation

Harold E. Cross; Ronald C. Hansen; Grant Morrow; John R. Davis

doi:10.1016/0002-9394(77)90450-0

Retinoblastoma in a patient with a 13qXp translocation

Harold E. Cross
, Ronald C. Hansen
, Grant Morrow
, John R. Davis

Ophthalmology and Vision Sciences

Research output: Contribution to journal › Article › peer-review

48 Scopus citations

Abstract

An infant girl with failure to thrive and bilateral retinoblastoma had a translocation of the long arm of chromosome 13 to the short arm of the X chromosome, and possible loss of a portion of the q14 band. The lack of other major organ malformations in this patient emphasized the importance of considering chromosomal aberrations as a possible etiology of retinoblastoma in patients with nonspecific psychomotor retardation.

Original language	English (US)
Pages (from-to)	548-554
Number of pages	7
Journal	American Journal of Ophthalmology
Volume	84
Issue number	4
DOIs	https://doi.org/10.1016/0002-9394(77)90450-0
State	Published - Oct 1977

ASJC Scopus subject areas

Ophthalmology

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10.1016/0002-9394(77)90450-0

Cite this

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title = "Retinoblastoma in a patient with a 13qXp translocation",

abstract = "An infant girl with failure to thrive and bilateral retinoblastoma had a translocation of the long arm of chromosome 13 to the short arm of the X chromosome, and possible loss of a portion of the q14 band. The lack of other major organ malformations in this patient emphasized the importance of considering chromosomal aberrations as a possible etiology of retinoblastoma in patients with nonspecific psychomotor retardation.",

author = "Cross, \{Harold E.\} and Hansen, \{Ronald C.\} and Grant Morrow and Davis, \{John R.\}",

year = "1977",

month = oct,

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language = "English (US)",

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pages = "548--554",

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T1 - Retinoblastoma in a patient with a 13qXp translocation

AU - Cross, Harold E.

AU - Hansen, Ronald C.

AU - Morrow, Grant

AU - Davis, John R.

PY - 1977/10

Y1 - 1977/10

N2 - An infant girl with failure to thrive and bilateral retinoblastoma had a translocation of the long arm of chromosome 13 to the short arm of the X chromosome, and possible loss of a portion of the q14 band. The lack of other major organ malformations in this patient emphasized the importance of considering chromosomal aberrations as a possible etiology of retinoblastoma in patients with nonspecific psychomotor retardation.

AB - An infant girl with failure to thrive and bilateral retinoblastoma had a translocation of the long arm of chromosome 13 to the short arm of the X chromosome, and possible loss of a portion of the q14 band. The lack of other major organ malformations in this patient emphasized the importance of considering chromosomal aberrations as a possible etiology of retinoblastoma in patients with nonspecific psychomotor retardation.

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UR - https://www.scopus.com/pages/publications/0017761244#tab=citedBy

U2 - 10.1016/0002-9394(77)90450-0

DO - 10.1016/0002-9394(77)90450-0

M3 - Article

C2 - 910860

AN - SCOPUS:0017761244

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EP - 554

JO - American Journal of Ophthalmology

JF - American Journal of Ophthalmology

IS - 4

ER -

Retinoblastoma in a patient with a 13qXp translocation

Abstract

ASJC Scopus subject areas

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